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3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3H)-quinazolinone

Base Information
  • Chemical Name:3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3H)-quinazolinone
  • CAS No.:338967-87-6
  • Molecular Formula:C15H10Cl2N2O2S
  • Molecular Weight:353.229
  • Hs Code.:
  • European Community (EC) Number:686-925-6
  • DSSTox Substance ID:DTXSID50396940
  • Nikkaji Number:J2.568.467B
  • Wikidata:Q72466672
  • ChEMBL ID:CHEMBL1449747
  • Mol file:338967-87-6.mol
3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3H)-quinazolinone

Synonyms:Mdivi-1;mitochondrial division inhibitor-1

Suppliers and Price of 3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3H)-quinazolinone
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Mdivi 1
  • 10mg
  • $ 339.00
  • TRC
  • Mdivi-1
  • 10mg
  • $ 65.00
  • Tocris
  • Mdivi1 ≥98%(HPLC)
  • 10
  • $ 102.00
  • Tocris
  • Mdivi1 ≥98%(HPLC)
  • 50
  • $ 428.00
  • TCI Chemical
  • Mdivi-1
  • 50MG
  • $ 366.00
  • TCI Chemical
  • Mdivi-1
  • 10MG
  • $ 106.00
  • Sigma-Aldrich
  • Mdivi-1 ≥98% (HPLC), powder
  • 25mg
  • $ 232.00
  • Sigma-Aldrich
  • Mitochondrial Division Inhibitor, mdivi-1
  • 10mg
  • $ 109.15
  • Sigma-Aldrich
  • Mdivi-1 ≥98% (HPLC), powder
  • 5mg
  • $ 58.30
  • DC Chemicals
  • Mdivi-1 >98%
  • 250 mg
  • $ 600.00
Total 30 raw suppliers
Chemical Property of 3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3H)-quinazolinone
Chemical Property:
  • Melting Point:289 °C 
  • Boiling Point:522.5±60.0 °C(Predicted) 
  • PKA:9.91±0.20(Predicted) 
  • PSA:82.92000 
  • Density:1.57±0.1 g/cm3(Predicted) 
  • LogP:3.98980 
  • Storage Temp.:Store at -20°C 
  • Solubility.:DMSO: >20mg/mL 
  • XLogP3:4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:351.9840041
  • Heavy Atom Count:22
  • Complexity:465
Purity/Quality:

99%, *data from raw suppliers

Mdivi 1 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C=C(C(=C1)N2C(=O)C3=CC=CC=C3NC2=S)Cl)Cl
  • Description Mdivi 1 is a mitochondrial division inhibitor. It inhibits the GTPase activity of yeast, but not human, dynamin-1 (Dnm1; IC50 = ~1-10 μM for the recombinant yeast enzyme) and human dynamin-related protein 1 (DRP1) in A549 lung cancer cells when used at a concentration of 50 μM. Mdivi 1 (50 μM) inhibits mitochondrial fragmentation and DRP1 self-assembly induced by staurosporine in COS cells overexpressing DRP1. It induces apoptosis in, and inhibits colony formation of, A549 cells when used at concentrations of 25 and 50 μM, respectively. Mdivi 1 (1 μM) decreases doxorubicin-induced increases in infarct-to-risk ratios in a Langendorff isolated perfused rat heart model of ischemia-reperfusion injury. It reduces the severity of lung injury in a mouse model of LPS-induced acute lung injury when administered at a dose of 20 mg/kg.
  • Uses Mdivi-1 is an inhibitor of mitochondrial division DRP1 and Dynamin I. Mdivi-1 has been used:in embryonic thoracic aorta A7r5 cells to inhibit cell migration and proliferationin mitochondrial network reshaping and reactive oxygen species (ROS) production studies in oligodendrocyte precursor cells (OPCs)to induce mitochondrial damage in lung fibroblasts
Technology Process of 3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3H)-quinazolinone

There total 4 articles about 3-(2,4-dichloro-5-methoxyphenyl)-2-sulfanyl-4(3H)-quinazolinone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In N,N-dimethyl-formamide; at 20 ℃; for 15.5h;
DOI:10.3987/COM-12-S(N)109
Guidance literature:
Multi-step reaction with 3 steps
1: pyridine / dichloromethane / 0.33 h / 20 °C
2: hydrogen; palladium 10% on activated carbon / N,N-dimethyl-formamide / 12 h / 20 °C / 750.08 Torr
3: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 15.5 h / 20 °C
With pyridine; palladium 10% on activated carbon; hydrogen; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.3987/COM-12-S(N)109
Guidance literature:
Multi-step reaction with 2 steps
1: hydrogen; palladium 10% on activated carbon / N,N-dimethyl-formamide / 12 h / 20 °C / 750.08 Torr
2: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 15.5 h / 20 °C
With palladium 10% on activated carbon; hydrogen; 1,8-diazabicyclo[5.4.0]undec-7-ene; In N,N-dimethyl-formamide;
DOI:10.3987/COM-12-S(N)109
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